MRI features of 4 female patients with pyruvate dehydrogenase E1 alpha deficiency.
about
Missense variants in the middle domain of DNM1L in cases of infantile encephalopathy alter peroxisomes and mitochondria when assayed in Drosophila.The spectrum of pyruvate oxidation defects in the diagnosis of mitochondrial disorders.Phenotypic and Neuropathological Characterization of Fetal Pyruvate Dehydrogenase Deficiency.The aetiology of neonatal seizures and the diagnostic contribution of neonatal cerebral magnetic resonance imaging.Pyruvate dehydrogenase deficiency and the brain.
P2860
MRI features of 4 female patients with pyruvate dehydrogenase E1 alpha deficiency.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
MRI features of 4 female patients with pyruvate dehydrogenase E1 alpha deficiency.
@ast
MRI features of 4 female patients with pyruvate dehydrogenase E1 alpha deficiency.
@en
type
label
MRI features of 4 female patients with pyruvate dehydrogenase E1 alpha deficiency.
@ast
MRI features of 4 female patients with pyruvate dehydrogenase E1 alpha deficiency.
@en
prefLabel
MRI features of 4 female patients with pyruvate dehydrogenase E1 alpha deficiency.
@ast
MRI features of 4 female patients with pyruvate dehydrogenase E1 alpha deficiency.
@en
P2093
P2860
P1433
P1476
MRI features of 4 female patients with pyruvate dehydrogenase E1 alpha deficiency.
@en
P2093
Andrea L Gropman
Jodie M Martin
Johanna B Loewenstein
Nicholas Ah Mew
Uta Lichter-Konecki
P2860
P356
10.1016/J.PEDIATRNEUROL.2011.02.003
P577
2011-07-01T00:00:00Z